Evidence map›Paper›PMID 22346758›Full record

ArticlePLoS genetics2012

Familial identification: population structure and relationship distinguishability.

Rori V Rohlfs, Stephanie Malia Fullerton, Bruce S Weir

Abstract read
In one paragraph

Article in PLoS genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Forensic genetics through the lens of Lewontin: population structure, ancestry and race.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Review
  7. Article
  8. Weaving the Strands of Life (Human biology · 2020
    Review
  9. Donnelly (1983) and the limits of genetic genealogy.Theoretical population biology · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Rori V RohlfsDepartment of Integrative Biology, University of California Berkeley, Berkeley, California, USA. rrohlfs@berkeley.edu
Stephanie Malia Fullerton
Bruce S Weir

Funding

Genomic Health Care and the Medically UnderservedP50HG003374 · NHGRI · UNIVERSITY OF WASHINGTON · PI BURKE, WYLIE G. · 2004 to 2014
$9.8M
Theoretical Population Genetics SupplementR01GM075091 · NIGMS · UNIVERSITY OF WASHINGTON · PI WEIR, BRUCE S. · 2006 to 2020
$4.7M
TRAINING PROGRAM IN GENETICS GENERAL AND MEDICALT32GM007735 · NIGMS · UNIVERSITY OF WASHINGTON · PI THOMAS, JAMES H · 1985 to 2009
$3.8M
NHGRI NIH HHS P50 HG003374NIGMS NIH HHS R01 GM075091NIGMS NIH HHS R01 GM75091NIGMS NIH HHS T32 GM007735NIGMS NIH HHS T32 GM07735
6 · The paper itself

Abstract

With the expansion of offender/arrestee DNA profile databases, genetic forensic identification has become commonplace in the United States criminal justice system. Implementation of familial searching has been proposed to extend forensic identification to family members of individuals with profiles in offender/arrestee DNA databases. In familial searching, a partial genetic profile match between a database entrant and a crime scene sample is used to implicate genetic relatives of the database entrant as potential sources of the crime scene sample. In addition to concerns regarding civil liberties, familial searching poses unanswered statistical questions. In this study, we define confidence intervals on estimated likelihood ratios for familial identification. Using these confidence intervals, we consider familial searching in a structured population. We show that relatives and unrelated individuals from population samples with lower gene diversity over the loci considered are less distinguishable. We also consider cases where the most appropriate population sample for individuals considered is unknown. We find that as a less appropriate population sample, and thus allele frequency distribution, is assumed, relatives and unrelated individuals become more difficult to distinguish. In addition, we show that relationship distinguishability increases with the number of markers considered, but decreases for more distant genetic familial relationships. All of these results indicate that caution is warranted in the application of familial searching in structured populations, such as in the United States.

Indexed as

Forensic GeneticsAllelesBiometric IdentificationConfidence IntervalsCrimeCriminalsDatabases, Nucleic AcidData Interpretation, StatisticalDNA FingerprintingFamilyGene FrequencyHumansLikelihood FunctionsPopulationUnited States

Identifiers

PMID22346758
PMCPMC3276546

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.